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GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 5-140567-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=140567&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 140567,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_052909.5",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLEKHG4B",
"gene_hgnc_id": 29399,
"hgvs_c": "c.1328C>A",
"hgvs_p": "p.Ala443Glu",
"transcript": "NM_052909.5",
"protein_id": "NP_443141.4",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1627,
"cds_start": 1328,
"cds_end": null,
"cds_length": 4884,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000637938.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_052909.5"
},
{
"aa_ref": "A",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLEKHG4B",
"gene_hgnc_id": 29399,
"hgvs_c": "c.1328C>A",
"hgvs_p": "p.Ala443Glu",
"transcript": "ENST00000637938.2",
"protein_id": "ENSP00000490806.1",
"transcript_support_level": 5,
"aa_start": 443,
"aa_end": null,
"aa_length": 1627,
"cds_start": 1328,
"cds_end": null,
"cds_length": 4884,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_052909.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000637938.2"
},
{
"aa_ref": "A",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLEKHG4B",
"gene_hgnc_id": 29399,
"hgvs_c": "c.260C>A",
"hgvs_p": "p.Ala87Glu",
"transcript": "ENST00000283426.11",
"protein_id": "ENSP00000283426.6",
"transcript_support_level": 1,
"aa_start": 87,
"aa_end": null,
"aa_length": 1271,
"cds_start": 260,
"cds_end": null,
"cds_length": 3816,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000283426.11"
},
{
"aa_ref": "A",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLEKHG4B",
"gene_hgnc_id": 29399,
"hgvs_c": "c.2C>A",
"hgvs_p": "p.Ala1Glu",
"transcript": "ENST00000502646.1",
"protein_id": "ENSP00000422493.1",
"transcript_support_level": 1,
"aa_start": 1,
"aa_end": null,
"aa_length": 421,
"cds_start": 2,
"cds_end": null,
"cds_length": 1266,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000502646.1"
},
{
"aa_ref": "A",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLEKHG4B",
"gene_hgnc_id": 29399,
"hgvs_c": "c.1328C>A",
"hgvs_p": "p.Ala443Glu",
"transcript": "ENST00000924300.1",
"protein_id": "ENSP00000594359.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1626,
"cds_start": 1328,
"cds_end": null,
"cds_length": 4881,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924300.1"
},
{
"aa_ref": "A",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLEKHG4B",
"gene_hgnc_id": 29399,
"hgvs_c": "c.1205C>A",
"hgvs_p": "p.Ala402Glu",
"transcript": "ENST00000924301.1",
"protein_id": "ENSP00000594360.1",
"transcript_support_level": null,
"aa_start": 402,
"aa_end": null,
"aa_length": 1585,
"cds_start": 1205,
"cds_end": null,
"cds_length": 4758,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924301.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLEKHG4B",
"gene_hgnc_id": 29399,
"hgvs_c": "c.244-14308C>A",
"hgvs_p": null,
"transcript": "ENST00000924299.1",
"protein_id": "ENSP00000594358.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1044,
"cds_start": null,
"cds_end": null,
"cds_length": 3135,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924299.1"
}
],
"gene_symbol": "PLEKHG4B",
"gene_hgnc_id": 29399,
"dbsnp": "rs563445670",
"frequency_reference_population": 6.8683016e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.8683e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.09643056988716125,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.025,
"revel_prediction": "Benign",
"alphamissense_score": 0.1287,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.63,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.925,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_052909.5",
"gene_symbol": "PLEKHG4B",
"hgnc_id": 29399,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.1328C>A",
"hgvs_p": "p.Ala443Glu"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}